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Piperaquine Pharmacokinetics during Intermittent Preventive Treatment for Malaria in Pregnancy.
Chotsiri, Palang; Gutman, Julie R; Ahmed, Rukhsana; Poespoprodjo, Jeanne Rini; Syafruddin, Din; Khairallah, Carole; Asih, Puji B S; L'lanziva, Anne; Otieno, Kephas; Kariuki, Simon; Ouma, Peter; Were, Vincent; Katana, Abraham; Price, Ric N; Desai, Meghna; Ter Kuile, Feiko O; Tarning, Joel.
Afiliação
  • Chotsiri P; Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
  • Gutman JR; Malaria Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
  • Ahmed R; Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
  • Poespoprodjo JR; Malaria and Vector Resistance Laboratory, Eijkman Institute for Molecular Biology, Jakarta, Indonesia.
  • Syafruddin D; Mimika District Health Authority, Timika, Papua, Indonesia.
  • Khairallah C; Timika Malaria Research Programme, Papuan Health and Community Development Foundation, Timika, Papua, Indonesia.
  • Asih PBS; Centre for Child Health and Department of Child Health, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia.
  • L'lanziva A; Malaria and Vector Resistance Laboratory, Eijkman Institute for Molecular Biology, Jakarta, Indonesia.
  • Otieno K; Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
  • Kariuki S; Malaria and Vector Resistance Laboratory, Eijkman Institute for Molecular Biology, Jakarta, Indonesia.
  • Ouma P; Centers for Diseases Control and Prevention, Kisumu, Kenya.
  • Were V; Kenya Medical Research Institute, Centre for Global Health Research, Kisumu, Kenya.
  • Katana A; Kenya Medical Research Institute, Centre for Global Health Research, Kisumu, Kenya.
  • Price RN; Kenya Medical Research Institute, Centre for Global Health Research, Kisumu, Kenya.
  • Desai M; Kenya Medical Research Institute, Centre for Global Health Research, Kisumu, Kenya.
  • Ter Kuile FO; Centers for Diseases Control and Prevention, Nairobi, Kenya.
  • Tarning J; Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Article em En | MEDLINE | ID: mdl-33361303
ABSTRACT
Dihydroartemisinin-piperaquine (DP) is a long-acting artemisinin combination treatment that provides effective chemoprevention and has been proposed as an alternative antimalarial drug for intermittent preventive therapy in pregnancy (IPTp). Several pharmacokinetic studies have shown that dose adjustment may not be needed for the treatment of malaria in pregnancy with DP. However, there are limited data on the optimal dosing for IPTp. This study aimed to evaluate the population pharmacokinetics of piperaquine given as IPTp in pregnant women. Pregnant women were enrolled in clinical trials conducted in Kenya and Indonesia and treated with standard 3-day courses of DP, administered in 4- to 8-week intervals from the second trimester until delivery. Pharmacokinetic blood samples were collected for piperaquine drug measurements before each treatment round, at the time of breakthrough symptomatic malaria, and at delivery. Piperaquine population pharmacokinetic properties were investigated using nonlinear mixed-effects modeling with a prior approach. In total, data from 366 Kenyan and 101 Indonesian women were analyzed. The pharmacokinetic properties of piperaquine were adequately described using a flexible transit absorption (n = 5) followed by a three-compartment disposition model. Gestational age did not affect the pharmacokinetic parameters of piperaquine. After three rounds of monthly IPTp, 9.45% (95% confidence interval [CI], 1.8 to 26.5%) of pregnant women had trough piperaquine concentrations below the suggested target concentration (10.3 ng/ml). Translational simulations suggest that providing the full treatment course of DP at monthly intervals provides sufficient protection to prevent malaria infection. Monthly administration of DP has the potential to offer optimal prevention of malaria during pregnancy. (This study has been registered at ClinicalTrials.gov under identifier NCT01669941 and in the ISRCTN under number ISRCTN34010937.).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quinolinas / Malária Falciparum / Complicações Parasitárias na Gravidez / Malária / Antimaláricos Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quinolinas / Malária Falciparum / Complicações Parasitárias na Gravidez / Malária / Antimaláricos Idioma: En Ano de publicação: 2021 Tipo de documento: Article